2-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)pyridine

2-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)pyridine, identified by CAS 1971914-58-5, is a highly functionalized pyridine derivative. Its molecular structure features a fluorine atom, a trifluoromethyl group, and a pinacol boronate ester strategically positioned on the pyridine ring. This combination of functional groups renders it a valuable intermediate in various research and development applications. The pinacol boronate moiety is particularly adept for Suzuki-Miyaura cross-coupling reactions, facilitating the formation of new carbon-carbon bonds with aryl or heteroaryl halides. The trifluoromethyl group often confers distinct electronic and steric properties, which can influence the reactivity and potential biological activity of synthesized target molecules. This compound is strictly for Research Use Only (RUO).

• Handle with appropriate personal protective equipment, including chemical-resistant gloves, safety glasses or goggles, and a lab coat. Ensure use in a well-ventilated area or a certified chemical fume hood to prevent inhalation exposure. Avoid direct contact with skin and eyes. In the event of contact, immediately flush the affected area with copious amounts of water. Store the compound in a cool, dry place, securely sealed and away from incompatible materials. Always refer to the Safety Data Sheet (SDS) for comprehensive safety guidelines and emergency procedures prior to handling. This product is intended solely for research purposes and is not for human or animal therapeutic, diagnostic, or clinical use.